Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
  • C08G18/40—High-molecular-weight compounds
  • C08G18/48—Polyethers
  • C08G18/50—Polyethers having heteroatoms other than oxygen
  • C08G18/5021—Polyethers having heteroatoms other than oxygen having nitrogen
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/08—Processes
  • C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
• • G—PHYSICS
  • G02—OPTICS
  • G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
  • G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
  • G02B1/04—Optical elements characterised by the material of which they are made; Optical coatings for optical elements made of organic materials, e.g. plastics
  • G02B1/041—Lenses

Definitions

• the subject of the present invention is the use of polyurethane resins for the manufacture of impact-resistant optical lenses, optical lenses, in particular ophthalmic lenses, obtained by virtue of the use of these resins, and the method of manufacturing said lenses.
• optical lens is meant in particular ophthalmic lenses and lenses for optical instrument.
• ophthalmic lens lenses adapted to a spectacle frame to protect the eye and / or correct vision, these lenses being selected from afocal lenses, unifocal, bifocal, trifocal and progressive.
• substrate is meant the basic constituent transparent material of the optical lens and more particularly of the ophthalmic lens. This material serves as a support for the stacking of one or more treatments, and helps to create the corrective function of the lens in the case of a corrective ophthalmic lens.
• Treatment means any coating that may be in contact with the substrate, and / or with another coating, and may in particular be an anti-reflection coating, antifouling, anti-shock, anti-scratch and / or polarizing primer.
• a substrate, to fulfill its function, must have all of the following characteristics:
• thermosetting resins constituting the substrate of the optical lens must be easy to implement industrially.
• the polymerizable resin used according to the invention is particularly advantageous. Indeed, the constituent elements of this resin are miscible at room temperature and a low viscosity. These characteristics make it possible in particular to formulate the polyurethane by simply mixing the constituents at room temperature, and pouring the mixture into a suitable mold, at a temperature of 18 to 60 ° C., preferably 18 to 50 ° C., very preferably 20 to 40 ° C, even more preferably at room temperature.
• the manufacturing process is simple, fast, reproducible, and low economic cost, the heating cycles being short and at low temperatures.
• Thermosetting polyurethane resins are known to those skilled in the art, to be adapted to the manufacture of optical lenses, in particular because these resins generally have an acceptable impact resistance.
• US Pat. No. 6,127,505 describes a polyurethane-urea resin prepared from a prepolymer, obtained by mixing aliphatic or cycloaliphatic diisocyanate and a glycol, and aromatic diamine. The preparation of the prepolymer itself is carried out under heating conditions of between 100 ° C. and 140 ° C. for a period of 3 to 5 hours, and the mixture of the prepolymer with the amine requires at least one heating step at a temperature of temperature of the order of 75 ° C.
• the method of manufacturing optical lenses according to the present invention differs from the prior art in particular in that the step of mixing the two compositions for forming the thermosetting polyurethane resin and the baking step, are carried out at the same time. temperatures much lower than those used in the processes of the prior art.
• the method of manufacturing an optical lens according to the invention is therefore easier to implement and allows a significant economic gain.
• the optical lens substrate according to the invention also has excellent impact resistance, is easily stainable, and can be easily coated under customary conditions.
• This resin therefore constitutes a material of choice as a substrate of an optical lens, and more particularly as a substrate of an ophthalmic lens.
• a first object of the invention therefore relates to the use, for the manufacture of optical lenses, of a thermosetting polyurethane resin comprising:
• a part (I), corresponding to the isocyanate part, comprising:
• a part (II), corresponding to the alcohol part, comprising:
• Part (II) has a viscosity of between 900 and 2500 mPa.s, preferably between 900 and 1800 mPa.s inclusive, and part (I) has a viscosity of between 300 and 1000 mPa.s inclusive.
• component (b) provides from 5% to 15% inclusive, and preferably 10%, of urethane function with respect to all the isocyante functions present in part (I).
• the alkoxylated glycerol etherate is of formula (C): HO- (R] -O) ⁇ -CH2-CH (- (O-R2) m -OH) -CH 2 - ( OR 3 ) p-OH (C) in which: R 1, R 2 and R 3 , which are identical or different, independently of one another, represent a linear or branched (C 2 -C 4 ) alkylene group;
• n, m and p identical or different, independently of one another, represent an integer between 1 and 6 inclusive.
• R 1 , R 2 and R 3 identical, represent an ethylene group or an isopropylene group
• n and p identical, represent an integer between 1 and 3 inclusive.
• part (c) of part (II) of said resin comprises compounds of formula (C) in which:
• R 1, R 2 and R 3 which are identical, represent a propylene group
• part (d) comprises at least one polyalkoxylated tertiary diamine tetraol and / or triol of formula (D):
• R 4 , R 5 and R 6 which are identical or different, independently of one another represent a group of formula (Dl):
• R 9 and R 10 which are identical or different, independently of one another, represent a group chosen from ethylene 7-propylene and isopropylene; or and, v, identical or different, independently of each other, represent an integer between 0 and 3 inclusive, it being understood that u and v do not simultaneously represent the value 0;
• R 7 represents a hydrogen atom or a group R 4 as defined above;
• Rg represents a linear or branched (C 2 -C 4 ) alkylene group.
• R 8 represents an ethylene group
• R 4 , R 5 and R 6 are identical and defined as previously;
• R 7 is as defined above.
• R 9 and R 10 are different and defined as above.
• the portion (d) of the portion (II) of said resin comprises: i. at least one polyalkoxylated tertiary diamine tetraol of formula (D) in which: R 4 , R 5 , R 6 and R 7 , identical, each represent a group of formula (Dl) in which:
• R 9 represents an ethylene group
• R 5 and R 6 each represent a group of formula (Dl) in which: • R 9 represents an ethylene group or isopropylene;
• RJ 0 represents an isopropylene or ethylene group
• - R 7 represents a hydrogen atom
• - R 8 represents an ethylene group
• iii. and the ratio of (i) to (ii) is from 100/0 to 90/10 inclusive.
• the polyurethane resin comprises part (II) for which the ratio between part (c) and part (d) is between 70/30 and 95/5 inclusive, preferably between 75/25. and 90/10 inclusive, and very preferably is equal to 80/20.
• the molar ratio between the portion (I) and the portion (II) of said resin is between 0.95 and 1.1.
• thermosetting polyurethane resin used in accordance with the invention generates a substrate with a view to producing an optical lens, with high impact resistance.
• One of the critical points for obtaining a high-impact thermosetting material is to optimize the compromise between a high T g (glass transition temperature) of the material, and a good impact resistance of said material. Indeed, obtaining a high Tg is desired, in order to obtain a stiffness dii substrate that avoids deformation during the application of treatments; a high Tg is generally obtained by introducing into the resin rigid segments which relax at high Tg.
• Achieving the impact resistance characteristic is generally obtained by introducing into the resin soft chains which relax at low T g or by reducing the crosslinking density of the polymer material contained in the resin. Indeed, an increase in the crosslinking density of the polymer has the consequence of restricting the mobility of the polymer chains and leads to a decrease in the flexibility of the resin. This loss of flexibility results in a decrease in the impact resistance of the resin, due in particular to the fact that the capacity of the resin to absorb shocks by dissipation of the induced energy is reduced.
• the polyurethane resin used in accordance with the invention consists of two entities: part (I) and part (II), part (I) corresponding to the isocyanate part, and part (II) corresponding to the alcohol part and comprising in particular at least one polyalkoxylated tertiary diamine tetraol and / or triol
• the resin used according to the invention is therefore both highly crosslinked, has a high Tg, and against all odds, also has good impact resistance.
• the resin used in accordance with the invention is very simple to implement, especially because the elements that constitute it are miscible at room temperature and have a low viscosity making casting easy.
• the properties of the part (II) of the resin used according to the invention are particularly important for the lowering of the overall viscosity of the mixture part (I) + part (II).
• the resin used is the PX521HT resin sold by the company Axson.
• the polyurethane resin used according to the invention may also comprise additives conventionally used in thermosetting resins for molding.
• optical lenses in particular ophthalmic lenses, in proportions conventionally used.
• demoulding agents that can be used in the context of the invention, there may be mentioned in particular trimethylchlorosilane, chloromethyltrimethylsilane, chloropropyltrimethylsilane, chloromethyldodecyl dimethylsilane, (3,3-dimethylbutyl) dimethylcholosilane, hexamethyldisilazane, octamethyltetrasilazane, aminopropyldimethylpolydimethylsiloxane, 3-trimethoxysilylpropyloctadecyl dimethylammonium chloride, tetradecyldimethyl (3-trimethoxysilylpropyl) ammonium chloride, trimethylethoxysilane, and octadecyltrimethoxysilane.
• antioxidants that can be used, generally in proportions of up to 5% by weight relative to the total weight of the reagents, mention may be made especially of hindered and polyfunctional phenolic antioxidants.
• UV stabilizers there may be mentioned benzotriazoles.
• the subject of the invention is also an optical lens substrate, in particular an ophthalmic lens substrate, characterized in that it is capable of being obtained from a thermosetting polyurethane resin as defined above, said resin having been molded and then polymerized.
• the substrate according to the invention may be coated with various layers such as: anti-abrasion coating; primary adhesion; anti-reflective coating, anti-fouling coating, polarizing coating. It can also be colored using conventional techniques.
• the subject of the invention is also a simple and economical method of manufacturing an optical lens, in particular an ophthalmic lens, from the polyurethane resin obtained by the formulation of part (I) and part (II), characterized in that it comprises a step of manufacturing the substrate, in which the parts (I) and (II) of the resin as defined above are mixed at a temperature of between 18 ° C. and 60 ° C. inclusive, preferably between 18 ° C. C and 50 ° C inclusive, very preferably between 20 ° C. and 40 ° C. inclusive, a mold adapted for the production of optical lenses is filled with the resin obtained, said filling being carried out manually or mechanically, and then the resin placed in the mold is polymerized, preferably between 80 ° C. and 130 ° C. inclusive, and an annealing step is then carried out.
• the PX521HT resin is part of the formulation of the polyurethane resin as described above.
• This resin is obtained by polymerizing: a part (I), corresponding to the isocyanate part comprising: (a) methylene-bis-4,4'-isocyanatecyclohexane (H 12 MDI) 5 (b) the prepolymer obtained from the reaction between the propoxylated glycerol and methylene-bis-4,4'-diisocyanatecyclohexane (a), (b) being present in a molar ratio of 10% of urethane function with respect to all the isocyanate functions present in the part (I)
• a part (II), corresponding to the alcohol part, comprising at least: (c) alkoxylated glycerol propoxylate in its monomeric and oligomeric form, the ratio between the monomeric form and the oligomeric forms being between 99/1 and 90 / 10
• Parts (I) and (II) are homogenized and degassed separately under an inert atmosphere and at room temperature (about 20 ° C.). The following steps are then performed:
• Part (I) and part (II) are degassed and heated respectively in separate tanks I and II.
• the reactants are driven to the mixing head by gear pumps as well as by pressurizing the tanks (about 2-3 bars). Pipes supplying the reagents of the tanks to the "product collector” are also heated. Stoichiometry is obtained by adjusting the speed of rotation of each of the pumps. The total flow rate is adjusted by an adjusting knob acting simultaneously on the speed of rotation of the two gear pumps (the relative speed of the two pumps remains unchanged and therefore the stoichiometry is not changed).
• the assembly "collector product” and mixer constitutes the mixing head.
• the alcohols reactants (part (II)) and isocyanates (part (I)) are contacted and homogenized in the mixer called “statico-dynamic" by those skilled in the art.
• the mixer core is driven by a variable speed pneumatic turbine.
• CBI test (ANSI 780 standard)
• CBI is an instrumented ball drop test.
• CBI has 3 impactors
• the choice of impactor is determined by the equipment according to the characteristics of the tested glass. An impactor falls at the geometric center of the glass to be tested. The impact speed is 5 m / s.
• a sensor located in the ball measures at all times the applied force and bending of the glass. The physical quantity followed is the energy at any moment of the shock. When the glass breaks, at this precise moment, the software gives the breaking energy of the glass.
• the CBI achieves a single impact per glass, do not retest the glasses, the glass must break every time.
• Each glass has a value of breaking energy.
• a 6.35 mm diameter steel ball is projected onto the tested lens with a speed of 15OfVs.
• the lens passes the test if it does not break.

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• Chemical & Material Sciences (AREA)
• Physics & Mathematics (AREA)
• Health & Medical Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Organic Chemistry (AREA)
• General Physics & Mathematics (AREA)
• Optics & Photonics (AREA)
• Polyurethanes Or Polyureas (AREA)
• Casting Or Compression Moulding Of Plastics Or The Like (AREA)

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Applications Claiming Priority (2)

Publications (1)

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Citations (3)

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• 2004
  • 2004-10-26 FR FR0411405A patent/FR2877006B1/fr not_active Expired - Fee Related
• 2005
  • 2005-10-26 DE DE602005010742T patent/DE602005010742D1/de active Active
  • 2005-10-26 EP EP05815132A patent/EP1819748B1/de not_active Not-in-force
  • 2005-10-26 WO PCT/FR2005/002685 patent/WO2006045960A1/fr active Application Filing
  • 2005-10-26 AT AT05815132T patent/ATE412680T1/de not_active IP Right Cessation
  • 2005-10-26 US US11/718,002 patent/US20090209723A1/en not_active Abandoned

Patent Citations (3)

Non-Patent Citations (1)

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